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ALPHA INFUSION PUMP

K992551 Class II Traditional
Decision Date
1999-10-27
Sponsor / Applicant
Advanced Infusion, Inc.

Technical Specification

510(k) Submission ID K992551
Product Code MEB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1999-10-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALPHA INFUSION PUMP received FDA 510(k) clearance under submission number K992551, sponsored by Advanced Infusion, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1999-10-27.

Classification & Regulation

This clearance is catalogued under FDA product code MEB and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.